Literature DB >> 11846662

A tin hydride designed to facilitate removal of tin species from products of stannane-mediated radical reactions.

Derrick L J Clive1, Jian Wang.   

Abstract

The stannane 1, which is simple to prepare, behaves like the conventional reagents Bu3SnH and Ph3SnH in standard free radical reactions, but with the special characteristic that the tin-containing byproducts are easily and very largely removed by mild hydrolysis (LiOH-water-THF or TsOH-water-THF), which converts them into base-soluble (aqueous NaHCO3) materials. The performance of stannane 1 was evaluated for a range of radical reactions involving halides, selenides, Barton-McCombie deoxygenation, and enyne cyclization. In several cases the effectiveness of the workup procedure in removing tin species was monitored by 1H NMR.

Entities:  

Year:  2002        PMID: 11846662     DOI: 10.1021/jo010885c

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Design, synthesis and in vitro splicing inhibition of desmethyl and carba-derivatives of herboxidiene.

Authors:  Arun K Ghosh; Kai Lv; Nianchun Ma; Emilio L Cárdenas; Kerstin A Effenberger; Melissa S Jurica
Journal:  Org Biomol Chem       Date:  2016-05-18       Impact factor: 3.876

2.  Mild deoxygenation of aromatic ketones and aldehydes over Pd/C using polymethylhydrosiloxane as the reducing agent.

Authors:  Alexey Volkov; Karl P J Gustafson; Cheuk-Wai Tai; Oscar Verho; Jan-E Bäckvall; Hans Adolfsson
Journal:  Angew Chem Int Ed Engl       Date:  2015-02-26       Impact factor: 15.336

Review 3.  Dihydronaphthofurans: synthetic strategies and applications.

Authors:  Abolfazl Olyaei; Mahdieh Sadeghpour
Journal:  RSC Adv       Date:  2020-02-05       Impact factor: 4.036

  3 in total

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